MAB21L1 protein [Bos taurus]

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External genitalia phenotypes of a Mab21l1-null mouse model for cerebellar, ocular, craniofacial, and genital (COFG) syndrome. [Anat Rec (Hoboken). 2024]
External genitalia phenotypes of a Mab21l1-null mouse model for cerebellar, ocular, craniofacial, and genital (COFG) syndrome.
Promsut W, Yamada R, Takami S, Miyazaki N, Uemura M, Hiramatsu R, Takahashi N, Kanai Y. Anat Rec (Hoboken). 2024 May; 307(5):1943-1959. Epub 2023 Sep 26.
Missense Mutations in MAB21L1: Causation of Novel Autosomal Dominant Ocular BAMD Syndrome. [Invest Ophthalmol Vis Sci. 2023]
Missense Mutations in MAB21L1: Causation of Novel Autosomal Dominant Ocular BAMD Syndrome.
Wang P, Wu P, Wang J, Zeng Y, Jiang Y, Wang Y, Li S, Xiao X, Zhang Q. Invest Ophthalmol Vis Sci. 2023 Mar 1; 64(3):19.
Structural and biochemical characterization of the cell fate determining nucleotidyltransferase fold protein MAB21L1. [Sci Rep. 2016]
Structural and biochemical characterization of the cell fate determining nucleotidyltransferase fold protein MAB21L1.
de Oliveira Mann CC, Kiefersauer R, Witte G, Hopfner KP. Sci Rep. 2016 Jun 8; 6:27498. Epub 2016 Jun 8.

RefSeq protein
See the reference protein sequence for putative nucleotidyltransferase MAB21L1 (NP_001091579.1).

Nucleotide
Nucleotide sequence from coding region
Taxonomy
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BioSystems
BioSystems
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

MAB21L1 protein [Bos taurus]
MAB21L1 protein [Bos taurus]
gi|133777583|gb|AAI23604.1|

Protein
Gene Links for Nucleotide (Select 13111796) (1)
Gene
SLC12A9 solute carrier family 12 member 9 [Homo sapiens]
SLC12A9 solute carrier family 12 member 9 [Homo sapiens]
Gene ID:56996

Gene

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Protein